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Gene|June 19, 1998
Diversity of sequence haplotypes associated with beta-thalassaemia mutations in Algeria: implications for their originP Perrin, R Bouhassa, L Mselli, et al.
Human Genetics|August 1, 1988
DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterizationF Rouabhi, C Lapouméroulie, S Amselem, et al.
Haematologia|January 1, 1983
New antisickling agentsD Labie
Pathologie-Biologie|November 1, 1975
[Molecular evolution]D Labie
La Revue Du Praticien|October 1, 1992
[Genetic aspects of sickle cell anemia]D Labie
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992
[Pathology of unstable sequence of genome: fragile-X-syndrome]C Beldjord, L Richard
Biochimie|January 1, 1975
Abnormal hemoglobin synthesis in some leukemic patientsJ Pagnier, D Labie
Hemoglobin|May 1, 1996
Sequence polymorphisms of potential functional relevance in the beta-globin gene locusD Labie, J Elion
Annales De Medecine Interne|January 1, 1981
[Recent data in the biology of sickle cell disease (author's transl)]H Wajcman, D Labie
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